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Microbially promoted calcite precipitation in the pelagic redoxcline: elucidating the formation of the turbid layer
Citation Link: https://doi.org/10.15480/882.4440
Publikationstyp
Journal Article
Publikationsdatum
2022-05-05
Sprache
English
Author
Leberecht, Kerstin
Lapp, Christian Jonas
Institut
Enthalten in
Volume
20
Issue
4
Start Page
498
End Page
517
Citation
Geobiology 20 (4): 498-517 (2022-07)
Publisher DOI
Scopus ID
Publisher
Wiley-Blackwell
Large bell-shaped calcite formations called “Hells Bells” were discovered underwater in the stratified cenote El Zapote on the Yucatán Peninsula, Mexico. Together with these extraordinary speleothems, divers found a white, cloudy turbid layer into which some Hells Bells partially extend. Here, we address the central question if the formation of the turbid layer could be based on microbial activity, more specifically, on microbially induced calcite precipitation. Metagenomic and metatranscriptomic profiling of the microbial community in the turbid layer, which overlaps with the pelagic redoxcline in the cenote, revealed chemolithoautotrophic Hydrogenophilales and unclassified ß-Proteobacteria as the metabolic key players. Bioinformatic and hydrogeochemical data suggest chemolithoautotrophic oxidation of sulfide to zero-valent sulfur catalyzed by denitrifying organisms due to oxygen deficiency. Incomplete sulfide oxidation via nitrate reduction and chemolithoautotrophy are both proton-consuming processes, which increase the pH in the redoxcline favoring authigenic calcite precipitation and may contribute to Hells Bells growth. The observed mechanism of microbially induced calcite precipitation is potentially applicable to many other stagnant sulfate-rich water bodies.
Schlagworte
biogeochemistry
chemolithoautotrophy
microbially induced calcite precipitation
redoxcline
sulfide oxidation
DDC Class
570: Biowissenschaften, Biologie
600: Technik
Projekt(e)
More Funding Information
This research has been supported by the Deutsche LEBERECHT et al. | 515 Forschungsgemeinschaft (grants no. STI128/28 and STI128/36) and the CONACYT-FONCICYT-DADC (grant no. 000000000278227).
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